Swevers Luc, Kravariti Lara, Ciolfi Silvia, Xenou-Kokoletsi Magda, Ragoussis Nikitas, Smagghe Guy, Nakagawa Yoshiaki, Mazomenos Bassilis, Iatrou Kostas
Institute of Biology, National Centre for Scientific Research Demokritos, P.O. Box 60228, Aghia Paraskevi Attikis, 153 10 Athens, Greece.
FASEB J. 2004 Jan;18(1):134-6. doi: 10.1096/fj.03-0627fje. Epub 2003 Nov 20.
Screening systems for ecdysteroid mimetic or antiecdysteroid substances in plant extracts or libraries of synthetic compounds are commonly based on the observation of morphological and/or growth responses in insect cell lines. Because these responses are slow and require careful monitoring, existing screening systems are considered limited regarding their applicability to analysis in high-throughput (HT) formats. Here we describe the generation of transformed silkmoth (Bombyx mori) cell lines that respond to the addition of ecdysone-like substances through the expression of the green fluorescent protein (GFP) and the appearance of green fluorescence. Because tests consist of three simple steps, i.e., 1) distribution of transformed cells in microtiter plates; 2) addition of compounds/extracts at different concentrations; and 3) quantification of fluorescence intensity by a fluorescence plate reader, they can be performed quickly and be easily adapted to a HT format. The generated reporter cell lines are used for the screening of extracts from available plant collections for the presence of compounds with ecdysone mimetic or antagonistic activities as well as for monitoring subsequent activity during enrichment and purification steps. The same cell lines are also used here for the determination of structure-activity relationships among available synthetic dibenzoylhydrazine derivatives. Finally, for the identified agonists, we show that their activity as determined by the cell-based screening assays parallels their bioactivity in growth inhibition and toxicity assays carried out on live insects.
用于筛选植物提取物或合成化合物文库中蜕皮甾体类似物或抗蜕皮甾体物质的系统通常基于对昆虫细胞系形态和/或生长反应的观察。由于这些反应缓慢且需要仔细监测,现有的筛选系统在高通量(HT)分析格式中的适用性被认为是有限的。在此,我们描述了转化家蚕(Bombyx mori)细胞系的产生,这些细胞系通过绿色荧光蛋白(GFP)的表达和绿色荧光的出现对蜕皮激素样物质的添加做出反应。由于测试包括三个简单步骤,即1)将转化细胞分布在微量滴定板中;2)添加不同浓度的化合物/提取物;3)用荧光酶标仪定量荧光强度,所以它们可以快速进行并且很容易适应高通量格式。所产生的报告细胞系用于筛选现有植物提取物中是否存在具有蜕皮激素模拟或拮抗活性的化合物,以及在富集和纯化步骤中监测后续活性。同样的细胞系在此还用于确定现有合成二苯甲酰肼衍生物之间的构效关系。最后,对于鉴定出的激动剂,我们表明基于细胞的筛选试验所确定的它们的活性与在活昆虫上进行的生长抑制和毒性试验中的生物活性相当。